journal of clinical research in pediatric endocrinology سال:2017 - دوره:9

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journal of clinical research in pediatric endocrinology
سال:2017 - دوره:9 - شماره:1

A rare cause of short stature: 3M syndrome in a patient with novel mutation in OBSL1 gene - صفحه:91-94 Age-specific frequencies and characteristics of ovarian cysts in children and adolescents - صفحه:58-62 Association between endocrine diseases and serous otitis media in children - صفحه:48-51 Clinical and molecular genetic analysis in three children with wolfram syndrome: A novel WFS1 mutation (c.2534T>A) - صفحه:80-84 Clinical and mutational features of three chinese children with congenital generalized lipodystrophy - صفحه:52-57 Comparison of updated weight and height percentiles with previous references in 6-17-year-old children in Kayseri,Turkey - صفحه:39-47 Follow-up findings in a Turkish girl with pseudohypoparathyroidism type ia caused by a novel heterozygous mutation in the GNAS gene - صفحه:74-79 Neck circumference to assess obesity in preschool children - صفحه:17-23 Non-classical congenital adrenal hyperplasia in childhood - صفحه:1-7 Role of versican and ADAMTS-1 in polycystic ovary syndrome - صفحه:24-30 Safety and efficacy of stosstherapy in nutritional rickets - صفحه:63-69 Subclinical hypothyroidism in danish lean and obese children and adolescents - صفحه:8-16 Testicular adrenal rest tumor in two brothers with a novel mutation in the 3-beta-hydroxysteroid dehydrogenase-2 gene - صفحه:85-90 The relationship between serum zonulin level and clinical and laboratory parameters of childhood obesity - صفحه:31-38 Uniparental isodisomy of chromosome 1 unmasking an autosomal recessive 3-beta hydroxysteroid dehydrogenase type II-related congenital adrenal hyperplasia - صفحه:70-73